A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15194097



Internal ID21332989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34506225..34506225hg38UCSC Ensembl
chr13:35080362..35080362hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951170
Supporting Variants
SamplesHG002
Known GenesLINC00457
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15194097
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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